Temporal Changes, Patient Characteristics, and Mortality, According to Microbiological Cause of Infective Endocarditis: A Nationwide Study

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Temporal Changes, Patient Characteristics, and Mortality, According to Microbiological Cause of Infective Endocarditis : A Nationwide Study. / Østergaard, Lauge; Voldstedlund, Marianne; Bruun, Niels Eske; Bundgaard, Henning; Iversen, Kasper; Køber, Nana; Christensen, Jens Jørgen; Rosenvinge, Flemming Schønning; Jarløv, Jens Otto; Moser, Claus; Andersen, Christian Østergaard; Coia, John; Marmolin, Ea Sofie; Søgaard, Kirstine K.; Lemming, Lars; Køber, Lars; Fosbøl, Emil Loldrup.

I: Journal of the American Heart Association, Bind 11, Nr. 16, e025801, 2022.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Østergaard, L, Voldstedlund, M, Bruun, NE, Bundgaard, H, Iversen, K, Køber, N, Christensen, JJ, Rosenvinge, FS, Jarløv, JO, Moser, C, Andersen, CØ, Coia, J, Marmolin, ES, Søgaard, KK, Lemming, L, Køber, L & Fosbøl, EL 2022, 'Temporal Changes, Patient Characteristics, and Mortality, According to Microbiological Cause of Infective Endocarditis: A Nationwide Study', Journal of the American Heart Association, bind 11, nr. 16, e025801. https://doi.org/10.1161/JAHA.122.025801

APA

Østergaard, L., Voldstedlund, M., Bruun, N. E., Bundgaard, H., Iversen, K., Køber, N., Christensen, J. J., Rosenvinge, F. S., Jarløv, J. O., Moser, C., Andersen, C. Ø., Coia, J., Marmolin, E. S., Søgaard, K. K., Lemming, L., Køber, L., & Fosbøl, E. L. (2022). Temporal Changes, Patient Characteristics, and Mortality, According to Microbiological Cause of Infective Endocarditis: A Nationwide Study. Journal of the American Heart Association, 11(16), [e025801]. https://doi.org/10.1161/JAHA.122.025801

Vancouver

Østergaard L, Voldstedlund M, Bruun NE, Bundgaard H, Iversen K, Køber N o.a. Temporal Changes, Patient Characteristics, and Mortality, According to Microbiological Cause of Infective Endocarditis: A Nationwide Study. Journal of the American Heart Association. 2022;11(16). e025801. https://doi.org/10.1161/JAHA.122.025801

Author

Østergaard, Lauge ; Voldstedlund, Marianne ; Bruun, Niels Eske ; Bundgaard, Henning ; Iversen, Kasper ; Køber, Nana ; Christensen, Jens Jørgen ; Rosenvinge, Flemming Schønning ; Jarløv, Jens Otto ; Moser, Claus ; Andersen, Christian Østergaard ; Coia, John ; Marmolin, Ea Sofie ; Søgaard, Kirstine K. ; Lemming, Lars ; Køber, Lars ; Fosbøl, Emil Loldrup. / Temporal Changes, Patient Characteristics, and Mortality, According to Microbiological Cause of Infective Endocarditis : A Nationwide Study. I: Journal of the American Heart Association. 2022 ; Bind 11, Nr. 16.

Bibtex

@article{81c2f3b0c9d24ba89b0dacb96706ffab,
title = "Temporal Changes, Patient Characteristics, and Mortality, According to Microbiological Cause of Infective Endocarditis: A Nationwide Study",
abstract = "BACKGROUND: Monitoring of microbiological cause of infective endocarditis (IE) remains key in the understanding of IE; how-ever, data from large, unselected cohorts are sparse. We aimed to examine temporal changes, patient characteristics, and in-hospital and long-term mortality, according to microbiological cause in patients with IE from 2010 to 2017. METHODS AND RESULTS: Linking Danish nationwide registries, we identified all patients with first-time IE. In-hospital and long-term mortality rates were assessed according to microbiological cause and compared using multivariable adjusted logistic re-gression analysis and Cox proportional hazard analysis, respectively. A total of 4123 patients were included. Staphylococcus aureus was the most frequent cause (28.1%), followed by Streptococcus species (26.0%), Enterococcus species (15.5%), coagulase-negative staphylococci (6.2%), and “other microbiological causes” (5.3%). Blood culture–negative IE was regis-tered in 18.9%. The proportion of blood culture–negative IE declined during the study period, whereas no significant changes were seen for any microbiological cause. Patients with Enterococcus species were older and more often had a prosthetic heart valve compared with other causes. For Streptococcus species IE, in-hospital and long-term mortality (median follow-up, 2.3 years) were 11.1% and 58.5%, respectively. Compared with Streptococcus species IE, the following causes were associated with a higher in-hospital mortality: S aureus IE (odds ratio [OR], 3.48 [95% CI, 2.74–4.42]), Enterococcus species IE (OR, 1.48 [95% CI, 1.11–1.97]), coagulase-negative staphylococci IE (OR, 1.79 [95% CI, 1.21–2.65]), “other microbiological cause” (OR, 1.47 [95% CI, 0.95–2.27]), and blood culture–negative IE (OR, 1.99 [95% CI, 1.52–2.61]); and the following causes were associated with higher mortality following discharge (median follow-up, 2.9 years): S aureus IE (hazard ratio [HR], 1.39 [95% CI, 1.19–1.62]), Enterococcus species IE (HR, 1.31 [95% CI, 1.11–1.54]), coagulase-negative staphylococci IE (HR, 1.07 [95% CI, 0.85–1.36]), “other microbiological cause” (HR, 1.45 [95% CI, 1.13–1.85]), and blood culture–negative IE (HR, 1.05 [95% CI, 0.89–1.25]). CONCLUSIONS: This nationwide study showed that S aureus was the most frequent microbiological cause of IE, followed by Streptococcus species and Enterococcus species. Patients with S aureus IE had the highest in-hospital mortality.",
keywords = "bloodstream infection, infective endocarditis, microbiological cause, nationwide study, population study",
author = "Lauge {\O}stergaard and Marianne Voldstedlund and Bruun, {Niels Eske} and Henning Bundgaard and Kasper Iversen and Nana K{\o}ber and Christensen, {Jens J{\o}rgen} and Rosenvinge, {Flemming Sch{\o}nning} and Jarl{\o}v, {Jens Otto} and Claus Moser and Andersen, {Christian {\O}stergaard} and John Coia and Marmolin, {Ea Sofie} and S{\o}gaard, {Kirstine K.} and Lars Lemming and Lars K{\o}ber and Fosb{\o}l, {Emil Loldrup}",
note = "Publisher Copyright: {\textcopyright} 2022 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.",
year = "2022",
doi = "10.1161/JAHA.122.025801",
language = "English",
volume = "11",
journal = "Journal of the American Heart Association",
issn = "2047-9980",
publisher = "Wiley-Blackwell",
number = "16",

}

RIS

TY - JOUR

T1 - Temporal Changes, Patient Characteristics, and Mortality, According to Microbiological Cause of Infective Endocarditis

T2 - A Nationwide Study

AU - Østergaard, Lauge

AU - Voldstedlund, Marianne

AU - Bruun, Niels Eske

AU - Bundgaard, Henning

AU - Iversen, Kasper

AU - Køber, Nana

AU - Christensen, Jens Jørgen

AU - Rosenvinge, Flemming Schønning

AU - Jarløv, Jens Otto

AU - Moser, Claus

AU - Andersen, Christian Østergaard

AU - Coia, John

AU - Marmolin, Ea Sofie

AU - Søgaard, Kirstine K.

AU - Lemming, Lars

AU - Køber, Lars

AU - Fosbøl, Emil Loldrup

N1 - Publisher Copyright: © 2022 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

PY - 2022

Y1 - 2022

N2 - BACKGROUND: Monitoring of microbiological cause of infective endocarditis (IE) remains key in the understanding of IE; how-ever, data from large, unselected cohorts are sparse. We aimed to examine temporal changes, patient characteristics, and in-hospital and long-term mortality, according to microbiological cause in patients with IE from 2010 to 2017. METHODS AND RESULTS: Linking Danish nationwide registries, we identified all patients with first-time IE. In-hospital and long-term mortality rates were assessed according to microbiological cause and compared using multivariable adjusted logistic re-gression analysis and Cox proportional hazard analysis, respectively. A total of 4123 patients were included. Staphylococcus aureus was the most frequent cause (28.1%), followed by Streptococcus species (26.0%), Enterococcus species (15.5%), coagulase-negative staphylococci (6.2%), and “other microbiological causes” (5.3%). Blood culture–negative IE was regis-tered in 18.9%. The proportion of blood culture–negative IE declined during the study period, whereas no significant changes were seen for any microbiological cause. Patients with Enterococcus species were older and more often had a prosthetic heart valve compared with other causes. For Streptococcus species IE, in-hospital and long-term mortality (median follow-up, 2.3 years) were 11.1% and 58.5%, respectively. Compared with Streptococcus species IE, the following causes were associated with a higher in-hospital mortality: S aureus IE (odds ratio [OR], 3.48 [95% CI, 2.74–4.42]), Enterococcus species IE (OR, 1.48 [95% CI, 1.11–1.97]), coagulase-negative staphylococci IE (OR, 1.79 [95% CI, 1.21–2.65]), “other microbiological cause” (OR, 1.47 [95% CI, 0.95–2.27]), and blood culture–negative IE (OR, 1.99 [95% CI, 1.52–2.61]); and the following causes were associated with higher mortality following discharge (median follow-up, 2.9 years): S aureus IE (hazard ratio [HR], 1.39 [95% CI, 1.19–1.62]), Enterococcus species IE (HR, 1.31 [95% CI, 1.11–1.54]), coagulase-negative staphylococci IE (HR, 1.07 [95% CI, 0.85–1.36]), “other microbiological cause” (HR, 1.45 [95% CI, 1.13–1.85]), and blood culture–negative IE (HR, 1.05 [95% CI, 0.89–1.25]). CONCLUSIONS: This nationwide study showed that S aureus was the most frequent microbiological cause of IE, followed by Streptococcus species and Enterococcus species. Patients with S aureus IE had the highest in-hospital mortality.

AB - BACKGROUND: Monitoring of microbiological cause of infective endocarditis (IE) remains key in the understanding of IE; how-ever, data from large, unselected cohorts are sparse. We aimed to examine temporal changes, patient characteristics, and in-hospital and long-term mortality, according to microbiological cause in patients with IE from 2010 to 2017. METHODS AND RESULTS: Linking Danish nationwide registries, we identified all patients with first-time IE. In-hospital and long-term mortality rates were assessed according to microbiological cause and compared using multivariable adjusted logistic re-gression analysis and Cox proportional hazard analysis, respectively. A total of 4123 patients were included. Staphylococcus aureus was the most frequent cause (28.1%), followed by Streptococcus species (26.0%), Enterococcus species (15.5%), coagulase-negative staphylococci (6.2%), and “other microbiological causes” (5.3%). Blood culture–negative IE was regis-tered in 18.9%. The proportion of blood culture–negative IE declined during the study period, whereas no significant changes were seen for any microbiological cause. Patients with Enterococcus species were older and more often had a prosthetic heart valve compared with other causes. For Streptococcus species IE, in-hospital and long-term mortality (median follow-up, 2.3 years) were 11.1% and 58.5%, respectively. Compared with Streptococcus species IE, the following causes were associated with a higher in-hospital mortality: S aureus IE (odds ratio [OR], 3.48 [95% CI, 2.74–4.42]), Enterococcus species IE (OR, 1.48 [95% CI, 1.11–1.97]), coagulase-negative staphylococci IE (OR, 1.79 [95% CI, 1.21–2.65]), “other microbiological cause” (OR, 1.47 [95% CI, 0.95–2.27]), and blood culture–negative IE (OR, 1.99 [95% CI, 1.52–2.61]); and the following causes were associated with higher mortality following discharge (median follow-up, 2.9 years): S aureus IE (hazard ratio [HR], 1.39 [95% CI, 1.19–1.62]), Enterococcus species IE (HR, 1.31 [95% CI, 1.11–1.54]), coagulase-negative staphylococci IE (HR, 1.07 [95% CI, 0.85–1.36]), “other microbiological cause” (HR, 1.45 [95% CI, 1.13–1.85]), and blood culture–negative IE (HR, 1.05 [95% CI, 0.89–1.25]). CONCLUSIONS: This nationwide study showed that S aureus was the most frequent microbiological cause of IE, followed by Streptococcus species and Enterococcus species. Patients with S aureus IE had the highest in-hospital mortality.

KW - bloodstream infection

KW - infective endocarditis

KW - microbiological cause

KW - nationwide study

KW - population study

U2 - 10.1161/JAHA.122.025801

DO - 10.1161/JAHA.122.025801

M3 - Journal article

C2 - 35946455

AN - SCOPUS:85136106591

VL - 11

JO - Journal of the American Heart Association

JF - Journal of the American Heart Association

SN - 2047-9980

IS - 16

M1 - e025801

ER -

ID: 319162258